Andersson K E, Bergdahl B, Dencker H, Wettrell G
Acta Pharmacol Toxicol (Copenh). 1977 Feb;40(2):280-4. doi: 10.1111/j.1600-0773.1977.tb02079.x.
In order to study the possibility that orally administered proscillaridin after absorption is transported by the lymph to the systemic circulation, the concentrations of the glycoside in thoracic duct lymph were analyzed in two patients with thoracic duct drainage. They received the drug as a single oral dose; plasma and lymph concentrations were measured by 86Rb-technique. Lymph was collected at various intervals for 24 hrs. The proscillaridin activity in thoracic duct lymph was low and followed closely that the plasma. During the sampling period, a total of 300 ng and 240 ng, respectively, was recovered in the lymph, corresponding to less than 0.03% of the administered dose. The results indicate that proscillaridin is not transported by the thoracic duct lymph.
为了研究口服海葱苷吸收后经淋巴转运至体循环的可能性,对两名胸导管引流患者胸导管淋巴中的糖苷浓度进行了分析。他们单次口服给药;采用86Rb技术测量血浆和淋巴浓度。在24小时内不同时间间隔收集淋巴。胸导管淋巴中海葱苷活性较低,且与血浆活性密切相关。在采样期间,淋巴中分别共回收了300纳克和240纳克,相当于给药剂量的不到0.03%。结果表明,海葱苷不是通过胸导管淋巴转运的。